(Q54280261)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:23222489%20AND%20SRC:MED&resulttype=core&format=json

19 February 2020

title

MED12 mutations in leiomyosarcoma and extrauterine leiomyoma (English)

1 reference

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19 February 2020

1 reference

9

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19 February 2020

Gloria Ravegnini

1

1 reference

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19 February 2020

author name string

Adrian Mariño-Enriquez

2

1 reference

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19 February 2020

Jaime Slater

3

1 reference

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19 February 2020

Grant Eilers

4

1 reference

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19 February 2020

Yuexiang Wang

5

1 reference

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19 February 2020

Meijun Zhu

6

1 reference

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19 February 2020

Marisa R Nucci

7

1 reference

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19 February 2020

Suzanne George

8

1 reference

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19 February 2020

Chandrajit P Raut

10

1 reference

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19 February 2020

Jonathan A Fletcher

11

1 reference

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19 February 2020

publication date

7 December 2012

1 reference

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19 February 2020

1 reference

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19 February 2020

volume

26

1 reference

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19 February 2020

issue

5

1 reference

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19 February 2020

page(s)

743-749

1 reference

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https://scigraph.springernature.com/pub.10.1038/modpathol.2012.203

19 February 2020

exact match

0 references

cites work

Uterine fibroids: the elephant in the room

1 reference

https://api.crossref.org/works/10.1038%2FMODPATHOL.2012.203

21 January 2018

Uterine sarcoma 2008.

1 reference

https://api.crossref.org/works/10.1038%2FMODPATHOL.2012.203

Clinical management of uterine sarcomas

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FMODPATHOL.2012.203

MED12, the mediator complex subunit 12 gene, is mutated at high frequency in uterine leiomyomas

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FMODPATHOL.2012.203

Whole exome sequencing in a random sample of North American women with leiomyomas identifies MED12 mutations in majority of uterine leiomyomas

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FMODPATHOL.2012.203

A unified nomenclature for protein subunits of mediator complexes linking transcriptional regulators to RNA polymerase II

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FMODPATHOL.2012.203

Cdk8 is essential for preimplantation mouse development

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FMODPATHOL.2012.203

Mutational analysis of MED12 exon 2 in uterine leiomyoma and other common tumors

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FMODPATHOL.2012.203

MED12 alterations in both human benign and malignant uterine soft tissue tumors

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FMODPATHOL.2012.203

The human CDK8 subcomplex is a histone kinase that requires Med12 for activity and can function independently of mediator

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FMODPATHOL.2012.203

Biallelic inactivation of fumarate hydratase (FH) occurs in nonsyndromic uterine leiomyomas but is rare in other tumors

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FMODPATHOL.2012.203

Genetic aberrations in soft tissue leiomyosarcoma

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FMODPATHOL.2012.203

Molecular and immunohistochemical evidence for the origin of uterine leiomyosarcomas from associated leiomyoma and symplastic leiomyoma-like areas.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FMODPATHOL.2012.203

Uterine leiomyosarcoma arising in leiomyoma: clinicopathological study of four cases and literature review.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FMODPATHOL.2012.203

Genetic heterogeneity among uterine leiomyomata: insights into malignant progression

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FMODPATHOL.2012.203

The original Lujan syndrome family has a novel missense mutation (p.N1007S) in the MED12 gene

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FMODPATHOL.2012.203

A novel mutation in MED12 causes FG syndrome (Opitz-Kaveggia syndrome).

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FMODPATHOL.2012.203

A recurrent mutation in MED12 leading to R961W causes Opitz-Kaveggia syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FMODPATHOL.2012.203

Exome sequencing identifies recurrent SPOP, FOXA1 and MED12 mutations in prostate cancer

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FMODPATHOL.2012.203

Pleomorphic soft tissue myogenic sarcomas of adulthood. A reappraisal in the mid-1990s

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FMODPATHOL.2012.203

7 January 2021

MED12 mutations in uterine fibroids--their relationship to cytogenetic subgroups

1 reference

https://api.crossref.org/works/10.1038%2FMODPATHOL.2012.203

7 January 2021

Uterine Fibroids and Evidence-Based Medicine — Not an Oxymoron

1 reference

https://api.crossref.org/works/10.1038%2FMODPATHOL.2012.203

7 January 2021

Molecular pathogenesis of uterine smooth muscle tumors from transcriptional profiling

1 reference

https://api.crossref.org/works/10.1038%2FMODPATHOL.2012.203

7 January 2021

Uterine myxoid leiomyosarcoma within a leiomyoma

1 reference

https://api.crossref.org/works/10.1038%2FMODPATHOL.2012.203

7 January 2021

Uterine leiomyosarcoma arising from a fibroid

1 reference

https://api.crossref.org/works/10.1038%2FMODPATHOL.2012.203

7 January 2021

Areas with benign morphologic and immunohistochemical features are associated with some uterine leiomyosarcomas

1 reference

https://api.crossref.org/works/10.1038%2FMODPATHOL.2012.203

7 January 2021